Benzyl (3-bromopropyl)carbamate

97%

  • Product Code: 118073
  CAS:    39945-54-5
Molecular Weight: 272.14 g./mol Molecular Formula: C₁₁H₁₄BrNO₂
EC Number: MDL Number: MFCD01737871
Melting Point: Boiling Point: 366.4°C at 760 mmHg
Density: 1.377g/cm3 Storage Condition: -20°C, dry sealed
Product Description: Used primarily in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for active compounds. The bromoalkyl group enables further functionalization through nucleophilic substitution reactions, making it useful in the creation of targeted drug molecules. Additionally, it finds application in the preparation of polymers and specialty chemicals, where its reactive sites allow for tailored modifications to achieve desired properties. Its role in peptide synthesis is also notable, as it can act as a protecting group for amines during multi-step reactions.
Product Specification:
Test Specification
Appearance White To Light Yellow To Yellow To Orange To Brown Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $71.18
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1.000 10-20 days $178.15
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5.000 10-20 days $688.99
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10.000 10-20 days $1,079.89
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Benzyl (3-bromopropyl)carbamate
Used primarily in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for active compounds. The bromoalkyl group enables further functionalization through nucleophilic substitution reactions, making it useful in the creation of targeted drug molecules. Additionally, it finds application in the preparation of polymers and specialty chemicals, where its reactive sites allow for tailored modifications to achieve desired properties. Its role in peptide synthesis is also notable, as it can act as a protecting group for amines during multi-step reactions.
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